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REAGENT / SYSTEM FOR PLATELET AGGREGATION - ANVISA Registration 80003610564

Access comprehensive regulatory information for REAGENT / SYSTEM FOR PLATELET AGGREGATION in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80003610564 and manufactured by ACCRIVA DIAGNOSTICS, INC.. The registration is held by WERFEN MEDICAL LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including HELENA LABORATORIES, ROCHE DIAGNOSTICS GMBH, and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.

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80003610564
Registration Details
ANVISA Registration Number: 80003610564
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Device Details

Registration Details

80003610564

25351555323201814

02004662000165

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Oct 08, 2018

VIGENTE

09/18/2025 19:00:01